Variant report

Variant	rs10911585
Chromosome Location	chr1:184335611-184335612
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs10911586	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12116705	0.97[EUR][1000 genomes]
rs12123538	0.95[EUR][1000 genomes]
rs12131730	0.87[EUR][1000 genomes]
rs12132220	0.83[EUR][1000 genomes]
rs12140904	0.95[EUR][1000 genomes]
rs12354368	0.97[EUR][1000 genomes]
rs13374592	0.89[EUR][1000 genomes]
rs17576899	0.97[EUR][1000 genomes]
rs17577247	0.97[EUR][1000 genomes]
rs56173711	0.89[EUR][1000 genomes]
rs60650088	0.89[EUR][1000 genomes]
rs6699949	0.84[EUR][1000 genomes]
rs9803754	0.96[AFR][1000 genomes];0.87[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs9804057	0.96[AFR][1000 genomes];0.87[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs9970469	0.97[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530079	chr1:183797938-184639971	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
2	nsv3821	chr1:184319543-184365236	Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:184332400-184335800	Weak transcription	Osteobl	bone
2	chr1:184332600-184336000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr1:184332800-184336000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr1:184332800-184336400	Weak transcription	Rectal Mucosa Donor 29	rectum
5	chr1:184333200-184336200	Weak transcription	Skeletal Muscle Female	skeletal muscle
6	chr1:184333800-184335800	Weak transcription	Fetal Muscle Leg	muscle
7	chr1:184333800-184336200	Weak transcription	Psoas Muscle	Psoas
8	chr1:184333800-184336800	Weak transcription	Skeletal Muscle Male	skeletal muscle

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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